510(k) K080582 ยท KPR System, X-Ray, Stationary
MEDICATECH, MODEL DDR MAK-800, DDT MAK-1000 FS, DDR MAK-1100 FA
| Applicant | Medicatech USA, Deer Field IL, US |
| Decision | Substantially Equivalent, May 15, 2008 |
| Received | Mar 3, 2008 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K080582
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.